JPH01136905A - Method for joining ferrous member - Google Patents
Method for joining ferrous memberInfo
- Publication number
- JPH01136905A JPH01136905A JP29278187A JP29278187A JPH01136905A JP H01136905 A JPH01136905 A JP H01136905A JP 29278187 A JP29278187 A JP 29278187A JP 29278187 A JP29278187 A JP 29278187A JP H01136905 A JPH01136905 A JP H01136905A
- Authority
- JP
- Japan
- Prior art keywords
- joining
- sintered alloy
- ferrous
- members
- ferrous sintered
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000005304 joining Methods 0.000 title claims abstract description 22
- 238000000034 method Methods 0.000 title claims abstract description 22
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 title claims abstract description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 26
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 20
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 20
- 239000000956 alloy Substances 0.000 claims abstract description 20
- 239000000463 material Substances 0.000 claims abstract description 18
- 229910002804 graphite Inorganic materials 0.000 claims abstract description 15
- 239000010439 graphite Substances 0.000 claims abstract description 15
- 239000007791 liquid phase Substances 0.000 claims abstract description 14
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 13
- 229910052742 iron Inorganic materials 0.000 claims abstract description 9
- 229910000831 Steel Inorganic materials 0.000 claims abstract description 6
- 239000010959 steel Substances 0.000 claims abstract description 6
- 238000010438 heat treatment Methods 0.000 claims abstract description 5
- 230000001590 oxidative effect Effects 0.000 claims abstract description 3
- 239000011248 coating agent Substances 0.000 claims description 8
- 238000000576 coating method Methods 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 238000002844 melting Methods 0.000 abstract 2
- 230000008018 melting Effects 0.000 abstract 2
- 238000003754 machining Methods 0.000 abstract 1
- 238000007796 conventional method Methods 0.000 description 6
- 239000002184 metal Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 238000005245 sintering Methods 0.000 description 4
- 238000005261 decarburization Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000008595 infiltration Effects 0.000 description 3
- 238000001764 infiltration Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 229910000975 Carbon steel Inorganic materials 0.000 description 2
- 238000005219 brazing Methods 0.000 description 2
- 239000010962 carbon steel Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- 229910000851 Alloy steel Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- 229910001096 P alloy Inorganic materials 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910001567 cementite Inorganic materials 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- KSOKAHYVTMZFBJ-UHFFFAOYSA-N iron;methane Chemical compound C.[Fe].[Fe].[Fe] KSOKAHYVTMZFBJ-UHFFFAOYSA-N 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000004881 precipitation hardening Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
Landscapes
- Powder Metallurgy (AREA)
Abstract
Description
【発明の詳細な説明】
この発明は、焼結技術を応用した鉄系部材の接合方法に
関するものであり、特に異なる材料を一体に構成した部
品を製造する場合に有用であり、例えば内燃機関用動弁
機構のバルブリフター、ロッカアーム等の製造に好適な
接合方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for joining iron-based members using sintering technology, and is particularly useful when manufacturing parts made of different materials, such as those for internal combustion engines. The present invention relates to a joining method suitable for manufacturing valve lifters, rocker arms, etc. of valve train mechanisms.
鉄鋼または鉄基焼結合金の要部に耐摩耗性結合合金のよ
うな別の材料を接合する場合、ろう付けが一般的である
が、その他加熱する最中に焼結合金から発生する液相に
より接合する方法、焼結材料に銅溶浸するとともにその
溶浸材で接合する方法、基材および接合する部材に凹凸
または適宜の底台形状を形成し、塑性加工により接合す
る方法、前記と同様に嵌合し加熱変形を利用して締まり
嵌め結合する方法等がある。When joining another material such as a wear-resistant bonding alloy to the main part of steel or iron-based sintered alloy, brazing is common, but other materials such as liquid phase generated from the sintered alloy during heating are used. A method of infiltrating a sintered material with copper and joining with the infiltrating material, a method of forming irregularities or an appropriate trapezoidal shape on the base material and the members to be joined, and joining by plastic working, and a method of joining by plastic working. There is also a method of fitting in a similar manner and utilizing thermal deformation to achieve tight fit and connection.
ところで一般に、各部材を訣め合い状態で接合するのに
比べ、積層状態で接合する場合は接合をより完全にしな
いと、繰り返し荷重により容易に分離されてしまう。By the way, in general, compared to joining each member in a tight state, when joining in a laminated state, unless the joining is more perfect, the members will easily separate due to repeated loads.
しかし従来技術において、積層接合面に嵌合する凹凸を
設けた機械的な接合方法は、使用する負荷が小さいもの
には適用できても高負荷または耐衝撃負荷がかかる機械
要素には不十分である。However, in the prior art, mechanical joining methods that provide unevenness that fits into the laminated joint surfaces are applicable to small loads, but are insufficient for machine elements that are subjected to high loads or shock-resistant loads. be.
その点、ろう付けは接合強度が高く接合信頼性も良いが
、焼結合金部材の空孔にろう材が溶浸し、多量のろう材
を要するとともに焼結材料の性質を変化させたり、作業
性が悪いという得失がある。In this regard, brazing has high bonding strength and good bonding reliability, but the filler metal infiltrates into the pores of the sintered metal parts, requiring a large amount of filler metal, changing the properties of the sintered material, and reducing workability. There are pros and cons to being bad.
溶浸接合法も上記と同様であって、溶浸材により封孔を
期待する場合は良いが、溶浸により焼結合金の性質を変
えたり、材料を多量に要し費用がかさむ欠点がある。The infiltration bonding method is similar to the above, and is good if sealing is expected with the infiltration material, but it has the disadvantages that infiltration changes the properties of the sintered alloy and requires a large amount of material, increasing costs. .
また、焼結合金の液相を利用した接合方法は、生産性が
良い反面、液相量が少ないために接合面の面粗さが大き
かったり、隙間があると接合が不完全になるとか、基部
材と接合部材の炭素dが異なるような場合、加熱中に炭
素が移動して要部を成す部材が変質するという問題点が
ある。In addition, although bonding methods that utilize the liquid phase of sintered alloys have good productivity, the amount of liquid phase is small, so the surface roughness of the bonded surface is large, and if there are gaps, the bond may be incomplete. If the carbon d of the base member and the bonding member are different, there is a problem that the carbon moves during heating and the main part of the member changes in quality.
この発明は上記した焼結材の液相を利用した接合方法を
改良したもので、その要旨は第1.第2部材の接合面に
黒鉛被膜を形成した後、各部材を組み合せ、無酸化雰囲
気中で加熱することを特徴とするものである。This invention is an improvement on the above-described joining method using the liquid phase of sintered materials, and the gist of this invention is as described in Section 1. The method is characterized in that after a graphite coating is formed on the joint surface of the second member, each member is assembled and heated in a non-oxidizing atmosphere.
以下本発明の構成および作用について説明する。The structure and operation of the present invention will be explained below.
まず、第1部材は部品の本体を形成し、鉄系焼結合金ま
たは溶製の鉄鋼月利である。この部材はありふれた亜共
析炭素鋼9合金鋼、耐熱鋼等、またはこれらに類似した
焼結合金であり、通常の機械要素用の鉄合金でおる。First, the first member forms the main body of the part and is made of a ferrous sintered alloy or a melted steel material. This member is made of common hypoeutectoid carbon steel 9 alloy steel, heat-resistant steel, etc., or a similar sintered alloy, and is made of an iron alloy for ordinary machine elements.
次に、第2部材は通常の焼結温度で液相を発生する金属
炭化物析出硬化型の耐摩耗性に優れた鉄系焼結合金でお
る。この発明の骨子は液相を生じる鉄系合金であれば、
同様な作用を示すが、産業上の適用が具体的で、最も効
果が大きい材料組み合せであることを考慮してこの焼結
材料が選択される。Next, the second member is made of a metal carbide precipitation hardening iron-based sintered alloy with excellent wear resistance that generates a liquid phase at normal sintering temperatures. The gist of this invention is that if the iron-based alloy produces a liquid phase,
Although it exhibits a similar effect, this sintered material is selected because it has a specific industrial application and is the most effective combination of materials.
この種の合金において、液相生成に寄与する元素はPが
挙げられる。その他にB、Sn、CLJ等を添加するこ
とがある。また、この合金は炭素を1〜4%程度含有し
ており、Feおよび後)ホする炭化物形成元素と結合す
る。炭化物形成元素としてCrは必須の元素で、Crは
鉄基地にも固溶し耐摩耗性に寄与する。In this type of alloy, P is an element that contributes to liquid phase formation. In addition, B, Sn, CLJ, etc. may be added. Further, this alloy contains about 1 to 4% carbon, which combines with Fe and carbide-forming elements. Cr is an essential element as a carbide-forming element, and Cr also dissolves in the iron matrix and contributes to wear resistance.
同様に炭化物を形成する元素でMO,W、V等を含んで
も良い。また、第2部材は圧粉体でも焼結体でも差し支
えない。Similarly, MO, W, V, etc. may be included as elements that form carbides. Further, the second member may be a compacted powder or a sintered body.
そこで、本発明者は次のような実験を行なった。Therefore, the inventor conducted the following experiment.
上記の如く第1部材と第2部材を従来法で接合、すなわ
ち、そのまま積み重ねて還元性ガス中、第2部材の液相
発生温度で加熱すると、焼結が進行するとともに、液相
が第2部材の接合面を濡らし、また、炭素は第2部材か
ら第1部材へ拡散する。As described above, when the first member and the second member are joined by the conventional method, that is, stacked as they are and heated in a reducing gas at the liquid phase generation temperature of the second member, sintering progresses and the liquid phase changes to the second member. The mating surfaces of the members are wetted and the carbon diffuses from the second member to the first member.
しかして、冷却した後の接合部近傍と各部材の情況を調
べてみると、従来法によれば、液相量が少ないために接
合部において細長い隙間が残存しており、また第2部材
は脱炭して硬さが低下し、さらに第1部材の接合部に近
い部分は浸炭した組織になっていることが判明した。However, when we investigated the situation near the joint and each member after cooling, we found that according to the conventional method, a long and narrow gap remained at the joint due to the small amount of liquid phase, and the second member It was found that the hardness decreased due to decarburization, and that the portion of the first member near the joint had a carburized structure.
これに対し、本発明方法は加熱する前に両部材の接合面
に黒鉛被膜を形成するものである。そのため黒鉛は接合
部において追加の液相を発生させ、また第2部材の脱炭
を防止する作用がある。また、この黒鉛被膜は適宜の分
散剤、粘性付与剤および消泡剤等を加えた水またはアル
コールのような分散媒に、コロイド状に黒鉛を分散させ
た塗料を塗布または吹付けた後、乾燥して得られる。塗
膜の厚さは1〜3μm程度が良い。塗膜が厚すぎると接
合面部にセメンタイトが多量に析出したり、未反応の黒
鉛が残存し、かえって疲労破壊し易くなる一方、1μm
以下では接合効果が劣るため、本願発明における黒鉛被
膜の厚さは1〜3μm程度が好ましい。In contrast, the method of the present invention forms a graphite coating on the joint surfaces of both members before heating. Therefore, graphite generates an additional liquid phase at the joint and also has the effect of preventing decarburization of the second member. In addition, this graphite film is created by coating or spraying a paint containing colloidal graphite dispersed in a dispersion medium such as water or alcohol containing appropriate dispersants, viscosity enhancers, antifoaming agents, etc., and then drying it. It can be obtained by The thickness of the coating film is preferably about 1 to 3 μm. If the coating film is too thick, a large amount of cementite will precipitate on the joint surface, and unreacted graphite will remain, making fatigue failure more likely.
If the thickness is below, the bonding effect will be poor, so the thickness of the graphite coating in the present invention is preferably about 1 to 3 μm.
このように、本発明方法に得られた接合部品の特徴は、
その断面を顕微鏡組織により観察することができる。そ
の結果、第1部材の接合部近傍は浸炭された組織を呈し
ていること、第2部材の脱炭がほとんどなく組成が均一
であること、および接合部は空孔が少なく、そこの炭素
量は第2部相接合部近傍と同じか僅かに多いことを観察
することができた。In this way, the characteristics of the joined parts obtained by the method of the present invention are as follows:
Its cross section can be observed under a microscope. As a result, we found that the vicinity of the joint of the first member has a carburized structure, that the second member has almost no decarburization and has a uniform composition, and that the joint has few pores and the amount of carbon therein. It could be observed that the number was the same or slightly higher than that near the second phase joint.
次に本発明の一実施例を従来法と比較して説明する。Next, an embodiment of the present invention will be described in comparison with a conventional method.
第1部材として0.2%Cの機械構造用炭素鋼を準備し
、接合する面を平面研削盤で研磨した。A 0.2% C carbon steel for mechanical structures was prepared as the first member, and the surfaces to be joined were ground with a surface grinder.
第2部材としてFe−C−Cr−Mo −W−V系のア
トマイズ合金鉄粉と、Fe−P合金粉、および黒鉛粉を
準備し、全体組成が重量比にて5%Cr−1,5%C−
3%MO−3%W−2%V−1,1%Pになるように配
合し、追加1%のステアリン酸亜鉛を加えて混合粉とし
、成形圧力6t/cMで所定形状に圧粉した後、温度1
000’Cの分解アンモニアガス雰囲気炉中で焼結した
。この焼結体の接合面も第1部材と同様に研磨した。As a second member, Fe-C-Cr-Mo-W-V-based atomized alloy iron powder, Fe-P alloy powder, and graphite powder were prepared, and the overall composition was 5% Cr-1,5 by weight. %C-
The mixture was blended to become 3% MO, 3% W, 2% V, and 1.1% P, and an additional 1% of zinc stearate was added to form a mixed powder, which was then pressed into a predetermined shape at a compacting pressure of 6 t/cM. After, temperature 1
Sintering was carried out in a decomposed ammonia gas atmosphere furnace at 000'C. The joint surface of this sintered body was also polished in the same manner as the first member.
この第2部材の一方には、接合面に水分散コロイド黒鉛
被膜を塗布、乾燥し、原ざ2μmの黒鉛被膜を形成させ
た(本発明)。さらに他の一方は研磨しただけの試料で
あって、従来法に属するものである。On one side of the second member, a water-dispersed colloidal graphite film was applied to the joint surface and dried to form a graphite film with a roughness of 2 μm (the present invention). Furthermore, the other one is a sample that has only been polished and belongs to the conventional method.
そこで、第1部材と第2部材はそれぞれの接合面を合せ
、温度1150°Cの分解アンモニアガス雰囲気炉中で
加熱処理した。そして得られた各試料について断面顕微
鏡組織および炭素量を調べた。Therefore, the first member and the second member were brought into contact with their joint surfaces and heat-treated in a decomposed ammonia gas atmosphere furnace at a temperature of 1150°C. The cross-sectional microstructure and carbon content of each sample obtained were examined.
その結果、黒鉛被膜を施した本発明に係る接合方法によ
れば試料の接合部には空孔が少なく良好に接着している
のに比べ、従来法による接合方法によれば両部材間に断
続的に隙間のあることが認められた。As a result, when using the bonding method according to the present invention in which a graphite coating was applied, there were few holes in the bonded part of the sample, and the bonding was good, whereas when using the conventional bonding method, there were no gaps between the two parts. It was recognized that there was a gap.
また、第1図は上記実験による接合部近傍の炭素量を示
したグラフであり、本発明に係る接合方法を実線、従来
法を点線で示している。このグラフから明らかなように
第1部材の浸炭深さは約1゜5mmで、本発明の方がや
や多い。また第2部材の炭素量は、従来法の場合間らか
に脱炭していることが認められ、本発明方法ではほとん
ど脱炭していないことがわかる。Further, FIG. 1 is a graph showing the amount of carbon near the joint according to the above experiment, in which the joining method according to the present invention is shown by a solid line, and the conventional method is shown by a dotted line. As is clear from this graph, the carburization depth of the first member is approximately 1.5 mm, which is slightly greater in the present invention. Further, it is recognized that the amount of carbon in the second member is gradually decarburized in the case of the conventional method, and it is found that the amount of carbon in the second member is hardly decarburized in the method of the present invention.
以上のような実験結果からも明らかなように、本発明に
係る接合方法によれば、要部の材質を変化させることな
く良好な接合が得られ、これを耐摩耗性複合部品の製造
方法に採用すれば、経済的で優れた接合品質を得ること
ができる。As is clear from the above experimental results, according to the joining method according to the present invention, good joining can be obtained without changing the material of the main parts, and this can be applied to the manufacturing method of wear-resistant composite parts. If adopted, it is possible to obtain economical and excellent bonding quality.
第1図は接合部品断面の炭素量を示したグラフである。 特許出願人 日立粉末冶金株式会社 FIG. 1 is a graph showing the amount of carbon in the cross section of the joined parts. Patent applicant Hitachi Powder Metallurgy Co., Ltd.
Claims (1)
第2部材が少なくともC,P,Crを含む鉄系焼結合金
からなる接合部品において、上記両部材の接合面に黒鉛
塗膜を形成した後両部材を組み合せ、無酸化雰囲気中で
第2部材の液相発生温度で加熱することを特徴とする鉄
系部材の接合方法。The first member is made of a ferrous sintered alloy or molten steel material,
In a jointed part in which the second member is made of an iron-based sintered alloy containing at least C, P, and Cr, a graphite coating film is formed on the joint surfaces of the above-mentioned two members, and then both members are combined, and the second member is assembled in a non-oxidizing atmosphere. A method for joining iron-based members, characterized by heating at a liquid phase generation temperature.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29278187A JPH07116493B2 (en) | 1987-11-19 | 1987-11-19 | Joining method for ferrous members |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29278187A JPH07116493B2 (en) | 1987-11-19 | 1987-11-19 | Joining method for ferrous members |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01136905A true JPH01136905A (en) | 1989-05-30 |
JPH07116493B2 JPH07116493B2 (en) | 1995-12-13 |
Family
ID=17786251
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP29278187A Expired - Lifetime JPH07116493B2 (en) | 1987-11-19 | 1987-11-19 | Joining method for ferrous members |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH07116493B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002236233A (en) * | 2000-11-27 | 2002-08-23 | Ibiden Co Ltd | Optical fiber array and method for manufacturing optical fiber array |
CN106471665A (en) * | 2014-07-02 | 2017-03-01 | 丰田自动车株式会社 | The method manufacturing lithium ion secondary battery electrode plate |
CN110293229A (en) * | 2019-07-05 | 2019-10-01 | 长飞光纤光缆股份有限公司 | A kind of graphene film-ferroalloy composite material and preparation method |
-
1987
- 1987-11-19 JP JP29278187A patent/JPH07116493B2/en not_active Expired - Lifetime
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002236233A (en) * | 2000-11-27 | 2002-08-23 | Ibiden Co Ltd | Optical fiber array and method for manufacturing optical fiber array |
CN106471665A (en) * | 2014-07-02 | 2017-03-01 | 丰田自动车株式会社 | The method manufacturing lithium ion secondary battery electrode plate |
CN110293229A (en) * | 2019-07-05 | 2019-10-01 | 长飞光纤光缆股份有限公司 | A kind of graphene film-ferroalloy composite material and preparation method |
CN110293229B (en) * | 2019-07-05 | 2020-06-19 | 长飞光纤光缆股份有限公司 | Graphene film-iron alloy composite material and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
JPH07116493B2 (en) | 1995-12-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5551413B2 (en) | Powder metal valve seat insert | |
US8157156B2 (en) | Powder metal friction stir welding tool and method of manufacture thereof | |
US4003715A (en) | Copper-manganese-zinc brazing alloy | |
JP5411334B2 (en) | Powder metal friction stir welding tool and manufacturing method thereof | |
JPH0210311B2 (en) | ||
JPH0258444B2 (en) | ||
JPS5830361B2 (en) | Method for manufacturing wear-resistant parts for internal combustion engines | |
US12169009B2 (en) | Friction brake body for a friction brake of a motor vehicle, method for producing a friction brake | |
JPS583902A (en) | Manufacture of cam shaft | |
CN107988595B (en) | Preparation of Fe by laser cladding3Al/Cr3C2Method for composite coating | |
JPS62243905A (en) | Rocker arm for internal combustion engine | |
JPH01136905A (en) | Method for joining ferrous member | |
US3886637A (en) | Method of producing heat treatable titanium carbide tool steel coatings on cylinders of internal combustion engines | |
US6712872B2 (en) | Powder metallurgy produced valve body and valve fitted with said valve body | |
KR100205795B1 (en) | Valve lifter and its mamufacturing method of internal combustion engine | |
US6534191B2 (en) | Sintered alloy and method for the hardening treatment thereof | |
KR100267709B1 (en) | A metal composition for engine valve seat, a method for manufacturing it, and an apparatus therefor | |
JPS62177184A (en) | Cast iron cylinder head for internal combustion engine and its production | |
KR20060037707A (en) | Flux for dissimilar metal melt bonding and dissociation method for dissimilar metal using same | |
Aso et al. | Surface hardening of cast iron inserted WC particles | |
JPH0374506A (en) | Manufacture of can tappet | |
JPH01186261A (en) | Joining method for valve seat | |
JPS60222513A (en) | Rocker arm | |
JP2839596B2 (en) | Method of manufacturing wear-resistant sliding member | |
JPH0152475B2 (en) |